Synthesis and Supramolecular Organization of para-Carboxyhydrazinylidene Derivative of 3-Nitrophenylthiazolo[3,2-a]pyrimidine

Synthesis of <i>para</i>-carboxyhydrazinylidene, the derivative of 3-nitrophenylthiazolo[3,2-<i>a</i>]pyrimidine, was successfully performed with good yields. It was established that different types of non-covalent intermolecular interaction may influence the supramolecular motif-synthesized compound. Hydrogen- and chalcogen-bonding supramolecular driving forces collectively impacted the results of two types of the centrosymmetric racemic dimeric self-assembly in crystalline phase.

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Published
2024-11-14
DOI
https://doi.org/10.3390/ecsoc-28-20101
Primary Topic
Synthesis and biological activity
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article
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article

Synthesis and Supramolecular Organization of para-Carboxyhydrazinylidene Derivative of 3-Nitrophenylthiazolo[3,2-a]pyrimidine

Alexander S. Ovsyannikov, Dilyara O. Mingazhetdinova, S. Е. Solovieva, Igor S. Antipin et al.
Synthesis and biological activity
article

Synthesis and Supramolecular Organization of para-Carboxyhydrazinylidene Derivative of 3-Nitrophenylthiazolo[3,2-a]pyrimidine

Alexander S. Ovsyannikov, Dilyara O. Mingazhetdinova, S. Е. Solovieva, Igor S. Antipin, Igor A. Litvinov, Anna A. Nefedova, Artem S. Agarkov
article en

Abstract

Synthesis of <i>para</i>-carboxyhydrazinylidene, the derivative of 3-nitrophenylthiazolo[3,2-<i>a</i>]pyrimidine, was successfully performed with good yields. It was established that different types of non-covalent intermolecular interaction may influence the supramolecular motif-synthesized compound. Hydrogen- and chalcogen-bonding supramolecular driving forces collectively impacted the results of two types of the centrosymmetric racemic dimeric self-assembly in crystalline phase.

Kazan Federal University (RU), A.E. Arbuzov Institute of Organic and Physical Chemistry (RU)
Clean water and sanitation
Openalex Percentile: Top 81%
Synthesis and biological activity
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Synthesis and Supramolecular Organization of para-Carboxyhydrazinylidene Derivative of 3-Nitrophenylthiazolo[3,2-a]pyrimidine — Alexander S. Ovsyannikov, Dilyara O. Mingazhetdinova, et al. · (2024) | TGRS Research Map | TGRS